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rs3180380

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3180380(C;C)
Make rs3180380(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356712
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3180380
ebirs3180380
HLIrs3180380
Exacrs3180380
Varsomers3180380
Maprs3180380
PheGenIrs3180380
hapmaprs3180380
1000 genomesrs3180380
hgdprs3180380
ensemblrs3180380
gopubmedrs3180380
geneviewrs3180380
scholarrs3180380
googlers3180380
pharmgkbrs3180380
gwascentralrs3180380
openSNPrs3180380
23andMers3180380
23andMe allrs3180380
SNP Nexus

SNPshotrs3180380
SNPdbers3180380
MSV3drs3180380
GWAS Ctlgrs3180380
GMAF0.1538
Max Magnitude0
ClinVar
Risk rs3180380(C,T;C,T)
Alt rs3180380(C,T;C,T)
Reference rs3180380(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324489C>A; NC_000006.11:g.31324489C>G
CLNSRC
CLNACC